HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 474321Generated: October 29, 2026
Cyclohexylamine → 5-chloro-N-cyclohexylpyrazolo[1,5-c]pyrimidine-3-carboxamide
https://huagongshe.com/reaction/474321
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cyclohexylamine | HCID 7965 | — |
| Reactant | 5-Chloropyrazolo[1,5-c]pyrimidine-3-carbonyl chloride | HCID 86661439 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-chloro-N-cyclohexylpyrazolo[1,5-c]pyrimidine-3-carboxamide | HCID 86661438 | 100% |
Reaction Steps
To a stirred solution of crude 5-chloropyrazolo[1,5-c]pyrimidine-3-carbonyl chloride (200 mg, 0.9 mM, 1.0 equiv) in 15 mL of dichloromethane was added cyclohexylamine (400 ul, 4.0 mM, 4 equiv). The reaction mixture was stirred for 15 minutes then quenched with 0.4 mL of acetic acid. The reaction mixture was concentrated under reduced pressure and the residue partitioned between water and dichloromethane. The dichloromethane phase was concentrated, and the crude product purified by flash chromatography on silica gel (97:3 dichloromethane:methanol) to yield 310 mg (100%) of 5-chloro-N-cyclohexylpyrazolo[1,5-c]pyrimidine-3-carboxamide. LCMS (ESI) m+H=279.1; 1H NMR (400 MHz, CDCl3) δ: 8.66 (s, 1H), 8.65 (d, 1H), 7.47 (d (broad exchangeable) 1H), 6.93 (d, 1H), 4.08 (m, 1H), 2.02 (m, 2H), 1.80 (m, 2H), 1.62 (m, 1H), 1.40 (m, 5H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08637526B2 |
|---|
| Source dataset | uspto-grants-2014_01 |
|---|
| ORD ID | ord-79952759a8004510b6356f8438a3c7b6 |
|---|
| Source note | uspto-grants-2014_01 |
|---|